1) RhoA kinase
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RhoA激酶
1.
Simvastatin prevents rat cardiac hypertrophy induced by myocardial infarction via RhoA kinase
辛伐他汀抑制心肌梗死后大鼠心肌细胞肥大与RhoA激酶关系
2) RhoA/Rho-kinase
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RhoA/Rho激酶
1.
Relationship Between RhoA/Rho-kinase Singaling Pathway and Penile Erection;
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RhoA/Rho激酶信号通路与阴茎勃起功能关系
2.
Effects of RhoA/Rho-kinase in the Regulation of Penile Erection;
![点击朗读](/dictall/images/read.gif)
RhoA/Rho激酶在阴茎勃起中的作用
3) RhoA/Rho kinase
![点击朗读](/dictall/images/read.gif)
RhoA/Rho激酶
1.
RhoA/Rho kinase:a potential new target for drug therapy in asthma and development of inhibitors
哮喘治疗新靶点——RhoA/Rho激酶及其抑制剂开发
2.
It has shown that vasoconstriction in the cavernosal circulation is mediated by the RhoA/Rho kinase calcium sensitization pathway.
阴茎海绵体血管的收缩及张力的维持是由钙敏感的RhoA/Rho激酶信号传导途径介导的。
3.
Objective:To investigate the role of RhoA/Rho kinase system in the onset of labor.
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目的:探讨子宫平滑肌组织RhoA/Rho激酶信号传导通路的表达变化在分娩发动中的作用。
5) kinase
[英]['kineis] [美]['kaɪ,nes, -,nez, 'kɪn,es, ,ez]
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激酶
1.
[Objective] The inhibitory effect of indirubin on cell growth was studied in some human tumor cell lines relating with cyclin-dependent kinases(CDK) or Src kinase.
[目的]探讨靛玉红对与细胞周期依赖性蛋白激酶(CDK)、Src激酶有关的人类肿瘤细胞生长的抑制作用。
2.
Purpose:To invastigate the changes of the related signaling pathways and it s mechanism of reguation of mitogen activated protein kinase cascade(MAPK) by SUM149 cells induced plasmid of dominant-negative E-cadherin mutant H-2k~d-E-cadherin.
1(-)H-2kd-E-cadherin)导入SUM149细胞系后,对丝裂原活化蛋白激酶信号传导系统(mitogenactivatedproteinkinasecascade,MAPK)的相关信号通路及调控机制的改变情况。
3.
Besides inhibiting protein Kinase C very well, they show potential bioactivities against Cyclin dependent kinase and Checkpoint kinase, and cell proliferation.
此类化合物对蛋白激酶C、细胞周期蛋白依赖激酶、检测点激酶等都具有较好的抑制作用 ,并能抑制肿瘤细胞增殖 ,因此可用于肿瘤的治
6) MAPK kinase kinase
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MAPK激酶激酶
1.
The conserved MAPK module includes three kinases that establish a sequential activation pathway comprising a MAPK, MAPK kinase ( MKK) and MAPK kinase kinase (MKKK).
MAPK途径的基本组合包括MAPK、MAPK激酶(MKK)和MAPK激酶激酶(MKKK)三种保守的成分,由此建立一个连续的激活途径。
补充资料:[3-(aminosulfonyl)-4-chloro-N-(2.3-dihydro-2-methyl-1H-indol-1-yl)benzamide]
分子式:C16H16ClN3O3S
分子量:365.5
CAS号:26807-65-8
性质:暂无
制备方法:暂无
用途:用于轻、中度原发性高血压。
分子量:365.5
CAS号:26807-65-8
性质:暂无
制备方法:暂无
用途:用于轻、中度原发性高血压。
说明:补充资料仅用于学习参考,请勿用于其它任何用途。
参考词条